JP6152785B2 - Lithium ion secondary battery - Google Patents

Description

  The present invention relates to a lithium ion secondary battery. Specifically, the present invention relates to a lithium ion secondary battery including a flat wound electrode body in a square case.

  Non-aqueous electrolyte secondary batteries such as lithium ion secondary batteries are used as so-called portable power sources such as personal computers and portable terminals, and vehicle driving power sources. In particular, a lithium ion secondary battery that is small, lightweight, and has a high energy density is preferably used as a driving power source for hybrid vehicles, electric vehicles, and the like.

  In a typical form of a lithium ion secondary battery, a flat wound electrode body and a non-aqueous electrolyte are accommodated in a rectangular rectangular case corresponding to the shape of the wound electrode body. By adopting such a configuration, it is possible to increase the capacity of each battery, and it is possible to efficiently arrange a large number of batteries in a limited space. For this reason, this form is preferably employed particularly in applications that require a high energy density (for example, a vehicle drive power supply).

Such a battery having a high energy density is generally used in a state where the voltage is controlled so as to be within a predetermined region (for example, 3.0 V to 4.2 V), but a current higher than usual is supplied by an erroneous operation or the like. In some cases, the battery may be overcharged exceeding a predetermined voltage. During such overcharge, gas may be generated due to decomposition of the non-aqueous electrolyte, or the temperature inside the battery may increase due to heat generation of the active material. As a technique for dealing with this problem, Patent Document 1 discloses a compound (typically an aromatic compound, hereinafter referred to as a “gas generating agent”) having a lower oxidative decomposition potential than a nonaqueous solvent in a nonaqueous electrolytic solution. Lithium ion secondary battery including a current interrupt device (CID: Current Interrupt Device) that forcibly cuts off the charging current when the pressure in the case exceeds a predetermined value due to decomposition of the gas generating agent. Is disclosed. When this battery is overcharged, the gas generating agent is oxidized and decomposed on the surface of the positive electrode, and hydrogen gas (H ₂ ) is generated at the negative electrode starting from this. The generated gas quickly increases the internal pressure of the battery, and the current interrupting mechanism can be activated early. For this reason, a battery with high reliability (overcharge tolerance) is realizable.

International Publication No. 2013/108396

By the way, in a lithium ion secondary battery like patent document 1, when the electric potential of a positive electrode becomes extremely high, elution of the metal element (typically transition metal element) which comprises a positive electrode active material locally, for example When the potential is exceeded, the metal element may be eluted from the positive electrode active material and deposited on the surface of the opposing separator or negative electrode. According to the knowledge of the present inventors, this may cause a minute short circuit in the battery and increase the self-discharge amount (leakage current).
The present invention has been made in view of such circumstances, and an object of the present invention is to prevent the potential of the positive electrode from becoming too high locally and to more reliably suppress elution of the metal element from the positive electrode active material. It is to provide a lithium ion secondary battery having a configuration that can be used.

As a result of detailed studies by the present inventors, elution of the metal element from the positive electrode active material is a “specific part”, that is, an end portion in the winding direction of the wound electrode body (in particular, on the winding center side). It was found that it is likely to occur at the starting end portion in the winding direction. Then, the present inventors considered suppressing the elution of the metal element in the edge part of the winding direction. As a result of further intensive studies, a means capable of solving the above problems has been found and the present invention has been completed.
That is, the lithium ion secondary battery provided by the present invention is a flat battery in which a long positive electrode and a long negative electrode longer than the positive electrode are stacked via a separator and wound in the longitudinal direction. The rotating electrode body and the nonaqueous electrolytic solution are accommodated in a square case. The wound electrode body has a negative electrode remainder protruding from the positive electrode at the winding center side in the winding direction at the start end in the winding direction on the winding center side. In addition, surplus nonaqueous electrolyte exists in the gap between the wound electrode body and the square case. The remainder of the negative electrode on the start end side is disposed in a region where the excess non-aqueous electrolyte exists when the battery is (regularly) disposed in a predetermined position at a predetermined position. Yes.

In the winding electrode body of a general lithium ion secondary battery, the negative electrode is longer than the positive electrode from the viewpoint of suppressing lithium deposition at the negative electrode at the start end of the winding electrode body in the winding direction. It protrudes to the winding center side in the winding direction. In other words, the negative electrode is a portion that does not face the positive electrode (hereinafter also simply referred to as “remainder portion”) and a portion that is in contact with the surplus portion at the start end in the winding direction located on the winding center side. A portion facing the positive electrode (hereinafter, also simply referred to as “opposing portion”).
In the negative electrode having such a configuration, lithium ions occluded by charging are gradually diffused from the facing portion to the surplus portion. According to the study by the present inventors, if air is present inside the square case at this time, lithium ions diffused in the remainder react with oxygen in the air to become lithium oxide. As a result, when the remaining portion of lithium ions is consumed, the lithium ions are further diffused from the facing portion to the remaining portion. When such a phenomenon continues, lithium ions are deficient in the facing portion, so that lithium ions can move excessively from the starting end portion of the positive electrode facing the facing portion. For this reason, the electric potential of the start end of the positive electrode is increased, and the elution of the metal element from the positive electrode active material can be accelerated locally at the site.

  Therefore, in the battery disclosed herein, the remainder of the negative electrode is disposed in the non-aqueous electrolyte (that is, below the liquid surface of the non-aqueous electrolyte). Thereby, even when oxygen is present inside the square case, the remainder of the negative electrode can be shielded from oxygen. Accordingly, it is difficult for lithium oxide to be generated at such sites, and the diffusion of lithium ions from the facing portion to the surplus portion can be reduced. That is, according to such a configuration, it is possible to prevent the potential at the starting end portion of the positive electrode facing the facing portion from being locally increased, and a metal element (typically a transition metal element, for example, a positive electrode active material). Elution of nickel (Ni), cobalt (Co), manganese (Mn), etc.).

  The internal structure of the battery (specifically, the positional relationship between the starting end of the positive electrode in the winding direction and the liquid level of the excess non-aqueous electrolyte) depends on the operating temperature range of the battery (typically the normal temperature range, For example, it can be clarified by performing nondestructive inspection measurement such as X-ray computed tomography (X-ray CT) in an environment of 25 ° C.

In a preferred aspect of the lithium ion secondary battery disclosed herein, the wound electrode body is wound at a winding outer peripheral side in the winding direction from the positive electrode at a terminal end in the winding direction on the wound outer peripheral side. The remainder of the negative electrode protruded. And the surplus part of the negative electrode on the terminal end side is arranged in a region where the surplus nonaqueous electrolyte is present.
In a typical configuration of the wound electrode body, not only the starting end portion in the winding direction but also a surplus portion of the negative electrode may exist at the terminal end portion (end portion on the wound outer peripheral side). In such a configuration, a local potential increase may occur at the end portion of the positive electrode in the winding direction as in the case of the start end portion. By making both the start and end portions of the negative electrode in the winding direction present in the non-aqueous electrolyte, local potential increase at the positive electrode end can be further suppressed, and the metal from the positive electrode active material can be suppressed. Element elution can be further suppressed. Therefore, the effect of the present invention can be exhibited at a higher level.

In a preferred aspect of the lithium ion secondary battery disclosed herein, the wound electrode body has two wound flat portions facing each other and a semicircular shape interposed between the two wound flat portions. It consists of two wound R sections. One of the two wound R portions is disposed on the bottom in the vertical direction of the square case when disposed in a predetermined posture at the predetermined position. And the starting end part of the winding direction of the said positive electrode and the liquid level of the said excess nonaqueous electrolyte solution are all arrange | positioned at the said winding flat part.
In general, since the wound R portion has a larger curvature than the wound flat portion, stress due to expansion / contraction of the active material layer accompanying charge / discharge is likely to be applied. In particular, since the radius of curvature is small at the start end of the positive electrode on the winding center side, the positive electrode active material layer may be cracked or the positive electrode active material layer may be peeled off. By disposing the start end portion of the positive electrode in the wound flat portion, such a problem can be prevented, and excellent battery characteristics can be stably realized. Further, the cost can be reduced by suppressing the height of the surplus non-aqueous electrolyte to the winding flat part as much as possible.

  In a preferred aspect of the lithium ion secondary battery disclosed herein, the remainder of the negative electrode on the start end side is disposed in the wound flat portion. In other words, the remainder of the negative electrode on the start end side is a wound flat part, and is sandwiched between the liquid surface of the nonaqueous electrolyte and the wound R part on the lower side (hereinafter also referred to as “lower R part”). Placed in the designated area. Thereby, the effect of the present invention can be exhibited at a higher level.

  In the present specification, the “bottom” refers to the side that is the lower side in the vertical direction of the rectangular case when the battery is placed in a predetermined position (regularly) in a predetermined position. Typically, it refers to the surface facing the lid of the square case. Therefore, “bottom” when the battery is temporarily in an irregular state due to, for example, rollover of the square battery or when the battery is assembled upside down is included in the bottom here. I can't.

  In a preferred aspect of the lithium ion secondary battery disclosed herein, the tip end of the positive electrode in the winding direction is positioned on the lower side in the vertical direction when the lithium ion secondary battery is disposed in the predetermined position at the predetermined position. It is suitable. According to such a configuration, the supply of oxygen to the remainder of the negative electrode can be more accurately blocked, and a battery with stable quality can be realized.

  In the present specification, the “starting end portion of the positive electrode in the winding direction” refers to a portion including the tip in the winding direction that is the most winding center side of the positive electrode. For example, it refers to a region including the tip and about several mm (for example, about 5 mm from the tip) in the winding direction.

In a preferred aspect of the lithium ion secondary battery disclosed herein, a current interruption mechanism that operates when the pressure in the square case increases, and decomposes to generate gas when the battery is overcharged. A gas generating agent.
As described above, in a battery containing a gas generating agent, for example, when the battery is stored in a state with a high state of charge (SOC), charging and discharging are repeated in a high temperature environment (for example, 50 ° C. to 70 ° C.). In some cases, the gas generating agent (typically an aromatic compound) is gradually oxidized and decomposed, and a polymer (polymer film) derived from the gas generating agent may be formed on the surface of the positive electrode. As a result, the structure of the positive electrode active material becomes unstable (for example, the valence of manganese element changes from Mn ^{2+ to} Mn ³⁺ ), and the elution potential of the metal element from the positive electrode may decrease. Alternatively, for example, when an aromatic gas generating agent is used, the aromatic compound may act like a catalyst to increase the reaction activity of the positive electrode active material, and the metal element may be easily eluted. Therefore, in the case of a battery including an additive (typically an aromatic compound such as a gas generating agent) that is oxidatively decomposed on the surface of the positive electrode and easily forms a polymer on the surface of the positive electrode, the application of the technology disclosed herein is particularly preferable. It is effective.

Further, according to the present invention, a flat wound electrode body in which a long positive electrode and a long negative electrode longer than the positive electrode are laminated via a separator and wound in the longitudinal direction, and non-aqueous Provided is a method for manufacturing a lithium ion secondary battery in which an electrolytic solution is housed in a square case. Such a manufacturing method is:
(1) Laminating the long positive electrode and the long negative electrode longer than the positive electrode through the separator and winding in the longitudinal direction to produce a flat wound electrode body, And the said winding electrode body has the negative electrode remainder part protruded in the winding center side of the winding direction rather than the positive electrode in the start end part in the winding direction in the winding center side;
(2) housing the wound electrode body in the square case;
(3) Injecting the non-aqueous electrolyte into the rectangular case in which the wound electrode body is housed, wherein the amount of the non-aqueous electrolyte is injected into the wound electrode body. The amount of excess nonaqueous electrolyte present in the gap between the wound electrode body and the square case that is impregnated with the nonaqueous electrolyte, and the negative electrode surplus portion on the start end side is the excess Determined to be vertically below the level of the non-aqueous electrolyte; and
(4) An initial charging process is performed between the positive electrode and the negative electrode in a state in which the negative electrode surplus portion on the start end side is disposed on the lower side in the vertical direction with respect to the liquid surface of the excess non-aqueous electrolyte. about;
Is included.

  According to the study by the present inventors, the elution of the metal element from the positive electrode active material as described above can be noticeably generated during the initial charging process (for example, aging after the first charging). By performing the initial charging process in a state where the negative electrode surplus portion on the start end side is disposed in the non-aqueous electrolyte, metal elution from the positive electrode active material can be effectively suppressed. Therefore, according to this manufacturing method, a lithium ion secondary battery with a reduced self-discharge amount can be efficiently and stably manufactured.

In a preferred aspect of the method for producing a lithium ion secondary battery disclosed herein, (1) the wound electrode body has a start end portion in the winding direction of the positive electrode disposed on two opposed wound flat portions. (2) When the wound electrode body is accommodated in the rectangular case, a semicircular shape is interposed between the two wound flat portions of the wound electrode body. One of the two winding R portions is disposed so as to be positioned at the bottom in the vertical direction of the square case when the battery is disposed at a predetermined position in a predetermined posture, and (3) the non-water The injection amount of the electrolytic solution is determined such that the height of the surplus nonaqueous electrolytic solution is positioned at the winding flat portion.
By arranging the starting end portion of the positive electrode in the winding direction in the winding flat portion, a wound electrode body having excellent mechanical strength can be stably realized. This is preferable in terms of reducing defective products (defective rate) in the manufacturing process. In addition, by arranging one of the winding R portions at the bottom of the square case in the vertical direction and adjusting the level of the nonaqueous electrolyte so that it comes to the winding flat portion, long-term durability and A battery having excellent reliability can be suitably manufactured.

  Such a lithium ion secondary battery can suppress the self-discharge amount (leakage current) because the elution of the metal element from the positive electrode active material is small even when the lithium ion secondary battery is held at a high temperature, for example. Therefore, taking advantage of such characteristics, it can be suitably used for, for example, applications that can be used in a wide temperature range and applications that require a high energy density. Examples of such applications include a power source (drive power source) for a motor mounted on a vehicle such as a plug-in hybrid vehicle (PHV). Therefore, as another aspect of the present invention, there is provided a vehicle including any of the lithium ion secondary batteries disclosed herein (which may be in the form of a battery pack).

It is a perspective view which shows typically the external shape of the lithium ion secondary battery which concerns on one Embodiment. It is a schematic diagram which shows the longitudinal cross-sectional structure which follows the II-II line | wire of FIG. It is a schematic diagram which shows the longitudinal cross-sectional structure which follows the III-III line | wire of FIG. It is a schematic diagram which shows the longitudinal cross-section of the lithium ion secondary battery which concerns on other one Embodiment. It is a figure which shows typically the longitudinal cross-section of lithium ion secondary battery B (comparative example). It is the graph which compared the elution amount of the metal element in the start end part of a wound electrode body.

  Hereinafter, preferred embodiments of the present invention will be described with reference to the drawings as appropriate. In addition, in the following drawings, the same code | symbol is attached | subjected to the member and site | part which show | plays the same effect | action, and the overlapping description may be abbreviate | omitted or simplified. The dimensional relationship (length, width, thickness, etc.) in each figure does not necessarily reflect the actual dimensional relationship. Further, matters other than matters specifically mentioned in the present specification and necessary for the implementation of the present invention can be grasped as design matters for those skilled in the art based on the prior art in this field. The present invention can be carried out based on the contents disclosed in this specification and common technical knowledge in the field.

Although not intended to be particularly limited, the present invention will be described in detail below by taking a lithium ion secondary battery according to an embodiment as an example.
A schematic configuration of a lithium ion secondary battery according to an embodiment of the present invention is shown in FIGS. FIG. 1 is a perspective view schematically showing the outer shape of the lithium ion secondary battery 100. FIG. 2 is a schematic view showing a longitudinal sectional structure taken along line II-II in FIG. FIG. 3 is a schematic view showing a longitudinal sectional structure taken along line III-III in FIG.

As shown in FIGS. 1 and 2, the lithium ion secondary battery 100 has a configuration in which a flat wound electrode body 80 and an excessive nonaqueous electrolyte solution 60 are accommodated in a square case 50.
The square case 50 includes a flat rectangular (rectangular) case main body 52 having an open upper end, and a lid 54 that closes the opening. As a material constituting the square case 50, a metal material such as aluminum or steel is preferably used. On the upper surface of the rectangular case 50 (that is, the lid 54), the positive terminal 70 for external connection that is electrically connected to the positive electrode 10 of the wound electrode body 80 and the negative electrode 20 of the wound electrode body 80 are electrically connected. A negative electrode terminal 72 to be connected is provided. The lid 54 is also provided with a safety valve 55 for discharging the gas generated inside the square case 50 to the outside of the square case 50.

  As shown in FIG. 2, a current interrupting mechanism 30 that operates by increasing the internal pressure of the rectangular case is provided inside the rectangular case 50. When the internal pressure of the square case 50 rises, the current interrupt mechanism 30 cuts a conductive path from at least one electrode terminal (that is, the positive terminal 70 and / or the negative terminal 72) to the wound electrode body 80. The charging current can be cut off. In this embodiment, the current interruption mechanism 30 is provided between the positive electrode terminal 70 fixed to the lid 54 and the wound electrode body 80, and is wound from the positive electrode terminal 70 when the internal pressure of the square case 50 rises. The conductive path reaching the electrode body 80 is cut.

Inside the rectangular case 50, a flat wound electrode body 80 and an excessive nonaqueous electrolyte solution 60 are accommodated. The space in the square case 50 is typically filled with dry air from the viewpoint of safety, cost, work efficiency, and the like. In other words, the space in the square case 50 can contain, for example, oxygen similar to that in the atmosphere.
The flat wound electrode body 80 includes a long sheet-like positive electrode (positive electrode sheet) 10 and a long sheet-like negative electrode (negative electrode sheet) 20. The positive electrode sheet 10 includes a long positive electrode current collector and a positive electrode active material layer formed on at least one surface (typically both surfaces) along the longitudinal direction. The negative electrode sheet 20 includes a long negative electrode current collector and a negative electrode active material layer formed on at least one surface (typically both surfaces) along the longitudinal direction. In addition, two separators 40 are disposed between the positive electrode active material layer and the negative electrode active material layer as an insulating layer that prevents direct contact therebetween.

  A positive electrode formed on the surface of the positive electrode current collector in the width direction defined as a direction from one end portion of the wound electrode body 80 toward the other end portion in the winding axis direction. A wound core portion is formed in which the active material layer and the negative electrode active material layer formed on the surface of the negative electrode current collector overlap and are densely stacked. Further, at both ends of the wound electrode body 80 in the winding axis direction, the positive electrode active material layer non-formed portion of the positive electrode sheet 10 and the negative electrode active material layer non-formed portion of the negative electrode sheet 20 are respectively outward from the wound core portion. It sticks out. A positive electrode current collector plate 74 is attached to the positive electrode side protruding portion (ie, the positive electrode active material layer non-forming portion), and a negative electrode current collector plate 76 is attached to the negative electrode side protruding portion (ie, the negative electrode active material layer non-forming portion). Each is electrically connected to the positive terminal 70 and the negative terminal 72 described above.

As shown in FIG. 3, the wound electrode body 80 includes the remainder of the negative electrode in which the negative electrode 20 protrudes from the positive electrode 10 to the winding center side in the winding direction at the winding-direction start end 81 on the winding center side. A portion 22 is provided. Accordingly, even when winding deviation occurs when the electrode body is wound, the positive electrode 10 can be prevented from protruding to the winding center side with respect to the negative electrode 20, and lithium deposition in the negative electrode 20 is preferable. Can be suppressed. The length (length in the winding direction) of the negative electrode surplus portion 22 at the start end portion 81 may be, for example, about several centimeters to several tens of centimeters. For example, in the embodiment shown in FIG. 3, the length of the remainder 22 of the negative electrode is about 4 cm (40 mm).
As in the case of the above-described start end portion 81, the wound electrode body 80 is typically wound in the winding direction at the end portion 83 in the winding direction on the winding outer peripheral side. It has a negative electrode remainder 24 that protrudes toward the outer periphery of the winding. The length (length in the winding direction) of the negative electrode surplus portion 24 at the terminal portion 83 of the wound electrode body 80 may be, for example, about several centimeters to several tens of centimeters. In the embodiment shown in FIG. 3, the length of the remainder 22 of the negative electrode is about 1 cm (10 mm).

  The separator 40 is typically in the form of a long sheet that is longer in the winding direction than the negative electrode 20. In the embodiment shown in FIG. 3, two separators 40 are used for one lithium ion secondary battery 100. One of the separators 40 has a surplus portion 42 corresponding to about 0.5 turns at the start end 81 in the winding direction on the winding center side of the wound electrode body 80, and the start end 21 of the negative electrode 20 and the positive electrode It is inserted between 10 start end portions 11. The other separator 40 has a surplus portion 42 for about 1.5 turns at the start end 81 in the winding direction on the winding center side of the wound electrode body 80, and the outer circumference of the circumference of the start end 11 of the positive electrode 10. It is sandwiched on the side. Further, the two separators 40 also have a separator surplus portion 44 protruding from the negative electrode 20 to the winding center side in the winding direction even at the winding end portion 83 on the winding outer periphery side of the winding electrode body 80. Have. The length (length in the winding direction) of the separator surplus portion 44 in the terminal portion 83 can be, for example, about several centimeters to several tens of centimeters. In the aspect shown in FIG. 3, the length of the separator surplus portion 44 is approximately 10 cm. Further, a winding tape is attached to the end portion 44 of the separator 40 so that the wound electrode body 80 is not unwound, and the shape of the wound electrode body 80 is maintained.

The wound electrode body 80 includes, in a cross section perpendicular to the winding axis, two wound flat portions 84 opposed to each other, and two semicircular wound R portions 82 interposed between the two wound flat portions. , 86. In this embodiment, one (lower R portion) 82 of the two wound R portions is arranged on the bottom in the vertical direction of the square case 50, and the other one (upper R) of the two wound R portions. Are disposed on the lid 54 side (ceiling side) in the vertical direction of the square case 50.
In a preferred embodiment, the starting end portion 11 in the winding direction of the positive electrode 10 is disposed on the winding flat portion 84. When the winding start end portion 11 of the positive electrode 10 is disposed in the winding R portions 82 and 86 having a high curvature, the positive electrode active material layer expands and contracts during charge and discharge, and high stress is applied to the portion, and the positive electrode active material The layer tends to peel easily. By adopting the above configuration, such a problem can be suitably prevented. In another preferred embodiment, the starting end portion 21 in the winding direction of the negative electrode is disposed on the winding flat portion 84. If it says dare, it is preferable that the remainder 22 of the negative electrode by the side of a start end part is arrange | positioned at the winding flat part 84. FIG. In other words, the entire starting end portion 81 in the winding direction of the wound electrode body 80 is preferably disposed on the wound flat portion 84. Thereby, it can prevent more reliably that a crack, slipping, etc. arise in the active material layer which exists near the winding center. Here, the “starting end portion of the negative electrode in the winding direction” refers to a portion including the tip in the winding direction that is the most winding center side of the negative electrode. For example, a region including the tip and an opposing portion that is in contact with the negative electrode surplus portion 22 and the negative electrode surplus portion in the winding direction from the leading end portion 11 in the winding direction of the positive electrode. Say.

  In the lithium ion secondary battery 100 disclosed herein, the non-aqueous electrolyte solution is impregnated in the wound electrode body 80, and an excess non-aqueous electrolyte solution is provided in the gap between the wound electrode body 80 and the square case 50. 60 exists. And the negative electrode surplus part 22 is arrange | positioned in the area | region where the excess non-aqueous electrolyte 60 exists, when a battery is arrange | positioned in a predetermined position in a predetermined position. In other words, the negative electrode surplus portion 22 is disposed on the lower side in the vertical direction than the liquid level 62 of the surplus non-aqueous electrolyte. By setting it as such a structure, it can prevent that the electric potential of the starting end part of a positive electrode becomes high too much locally, and can suppress the elution of the metallic element from a positive electrode active material.

  In a preferred embodiment, in addition to the negative electrode surplus portion 22, the positive electrode start end portion 11 is also disposed in a region where the surplus non-aqueous electrolyte 60 exists. In other words, it is arranged below the liquid level 62 of the surplus non-aqueous electrolyte in the vertical direction. The liquid surface height 62 of the non-aqueous electrolyte solution may vary slightly, for example, when the battery is tilted or when the temperature in the battery becomes high and the non-aqueous solvent component is vaporized. By arranging the negative electrode surplus portion 22 and the positive electrode start end portion 11 in a region where the excess non-aqueous electrolyte 60 exists, the negative electrode surplus portion 22 can be more reliably shielded from oxygen, and the oxygen source is cut off. Can do. Therefore, the production of lithium oxide in the remainder 22 of the negative electrode can be further suppressed, and the potential at the start end 11 of the positive electrode can be prevented from rising locally.

  In a preferred embodiment, when the battery is arranged at a predetermined position in a predetermined posture, the tip of the start end portion 11 in the winding direction of the positive electrode faces downward in the vertical direction. According to this aspect, the start end 81 in the winding direction of the wound electrode body 80 (typically, the negative electrode surplus portion 22 on the start end side, for example, the positive electrode start end 11 and the negative electrode start end 21) is more reliably provided. It can be arranged in a region where there is excess non-aqueous electrolyte 60.

In the technology disclosed herein, the negative electrode surplus portion 22 on the start end side is disposed in a region where the nonaqueous electrolyte solution 60 exists, as shown in FIGS. 3 and 4, for example. On the other hand, the remaining portion 24 of the negative electrode on the terminal end side may be disposed in a region where the non-aqueous electrolyte 60 is present, or may be disposed in a region where the non-aqueous electrolyte 60 is present.
For example, in the embodiment shown in FIG. 3, the negative electrode surplus portion 24 on the wound outer peripheral side of the wound electrode body 80 is disposed in a region where the excess non-aqueous electrolyte 60 exists. In other words, the surplus portion 22 on the start end side and the surplus portion 24 on the end portion side of the negative electrode are both disposed on the lower side in the vertical direction than the liquid level 62 of the surplus nonaqueous electrolyte. With such a configuration, it is possible to prevent the potential of the positive electrode from being locally increased at the start end portion and the end end portion, and the effects of the present invention can be exhibited at a high level.
Further, a lithium ion secondary battery 100a according to another embodiment shown in FIG. 4 includes a rectangular case 50a and a wound electrode body 80a, and is wound on the winding center side of the wound electrode body 80a. The start end 81a of the electrode body (typically, the negative electrode surplus portion 22a on the start end side, for example, the positive electrode start direction 11a and the negative electrode start direction 21a) is a surplus non-aqueous electrolyte. It is arranged in a region where 60a exists. In other words, the start end portion 81a of the wound electrode body is disposed on the lower side in the vertical direction than the liquid level 62a of the surplus nonaqueous electrolyte. On the other hand, the end portion 83a of the wound electrode body on the winding outer peripheral side of the wound electrode body 80a (typically, the remainder 24a of the negative electrode on the terminal end side, for example, the terminal portion 13a in the winding direction of the positive electrode and the negative electrode The end portion 23a) in the winding direction is arranged in a region where there is no excess nonaqueous electrolyte solution 60. Such a configuration can be preferably used particularly when the area of the remainder of the negative electrode is narrow (or almost absent) at the end portion 83a in the winding direction of the wound electrode body 80a.

  In a preferred embodiment, as shown in FIG. 3, the negative electrode surplus portion 24 on the wound outer peripheral side of the wound electrode body 80 is disposed in a region 60 where excess nonaqueous electrolyte is present. For example, the terminal portion 13 in the winding direction of the positive electrode and the terminal portion 23 in the winding direction of the negative electrode are both disposed below the liquid level 62 of the surplus nonaqueous electrolyte in the vertical direction. Thereby, the effect of the present invention can be exhibited at a high level.

  In the conventional general lithium ion secondary battery, the wound electrode body is impregnated with almost the entire amount of the nonaqueous electrolyte injected from the viewpoint of low cost. That is, there is no excess nonaqueous electrolyte in the gap between the wound electrode body and the square case, or a slight excess of nonaqueous electrolyte is confirmed when the case is tilted. . On the other hand, in the lithium ion secondary battery 100 disclosed herein, the above-described merits are obtained (that is, local increase in the positive electrode potential is suppressed and elution of the metal element from the positive electrode active material is suppressed. ) From the viewpoint, an excessive nonaqueous electrolytic solution 60 is provided.

In another preferable aspect, the liquid level 62 of the surplus non-aqueous electrolyte is disposed on the wound flat portion 84. As described above, it is preferable that the start end portion 11 in the winding direction of the positive electrode is disposed on the winding flat portion 84. For this reason, it is preferable that the liquid level 62 of excess electrolyte solution is higher than one R part (lower R part) 82 of the wound electrode body 80. Further, from the viewpoint of low cost, it is preferable that the liquid level 62 of the surplus electrolyte is lower than the other R portion (upper R portion) 86 of the wound electrode body 80.
In a preferred embodiment, the surplus electrolyte liquid level 62 may be approximately ¼ to ¾ of the height of the square case 50. In the embodiment shown in FIG. 3, the surplus electrolyte liquid level 62 is disposed at approximately half the height of the square case 50.

In addition, the material and member itself which comprise the lithium ion secondary battery 100 may be the same as that of a conventionally well-known lithium secondary battery, and are not specifically limited.
For example, as the rectangular case 50, a lightweight metal material such as aluminum can be preferably used. In a preferred embodiment, the square case 50 is provided with a current interrupting mechanism (CID) 30 that operates when the pressure in the case increases. Thereby, a high-capacity battery excellent in reliability (overcharge resistance) can be realized.

As the positive electrode 10 constituting the wound electrode body 80, a positive electrode active material was adhered to the surface of the positive electrode current collector as a composition together with a binder, a conductive material, etc., and a positive electrode active material layer was formed on the positive electrode current collector. The thing of a form can be used conveniently. As the positive electrode active material, a lithium composite metal oxide having a layered structure or a spinel structure (for example, LiNiO ₂ , LiCoO ₂ , LiFeO ₂ , LiMn ₂ O ₄ , LiNi _0.33 Co _0.33 Mn _0.33 O ₂ , LiNi _0.5 Mn _1.5 O ₄ , LiCrMnO ₄ , LiFePO ₄ ) and the like can be suitably employed. As the binder, a polymer material such as polyvinylidene fluoride (PVdF) or polyethylene oxide (PEO) can be suitably used. A carbon material such as carbon black (for example, acetylene black or ketjen black) can be suitably used as the conductive material. As the positive electrode current collector, a conductive member made of a metal having good conductivity (for example, aluminum) can be suitably employed.

As the negative electrode 20 constituting the wound electrode body 80, a negative electrode active material is adhered to the surface of the negative electrode current collector as a composition together with a binder, a thickener, etc., and a negative electrode active material layer is formed on the negative electrode current collector The thing of the form which was made can be used conveniently. As the negative electrode active material, a carbon material such as graphite (graphite), non-graphitizable carbon (hard carbon), graphitizable carbon (soft carbon), or the like can be used, and among them, graphite can be preferably used. As the binder, polymer materials such as polytetrafluoroethylene (PTFE) and rubbers such as styrene butadiene rubber (SBR) can be suitably used. As the thickener, cellulose such as carboxymethyl cellulose (CMC) can be suitably used. As the negative electrode current collector, a conductive material made of a metal having good conductivity (for example, copper) can be suitably used.
Further, the capacity ratio (C _N / C _P ) calculated as the capacity ratio of the positive and negative electrodes, that is, the ratio of the initial charge capacity (C _N ) of the negative electrode to the initial charge capacity (C _P ) of the positive electrode is, for example, 1.0 to 2.1. By setting it as the said range, a high energy density and the outstanding cycling characteristics are realizable.

As the separator 40 constituting the wound electrode body 80, a porous resin sheet made of a resin such as polyethylene (PE) or polypropylene (PP) can be suitably used. Among them, on one side or both sides of the porous resin sheet, alumina (aluminum oxide: Al 2 _{O 3)} or silica (silicon oxide: SiO ₂₎ which comprises a porous heat-resistant layer containing an inorganic filler such as is preferred. According to this form, even if the temperature in the battery rises for some reason (for example, 150 ° C. or higher, typically 200 ° C. or higher), the positive and negative insulating states are preferably Can be maintained. Further, even when lithium is deposited on the surface of the negative electrode due to repeated charge / discharge or the like, it is possible to suppress a minute short-circuit at the portion, and to reduce the amount of self-discharge.

As the non-aqueous electrolyte, a non-aqueous solvent containing a supporting salt can be suitably used. As the non-aqueous solvent, aprotic solvents such as carbonates, esters, ethers, nitriles, sulfones and lactones can be used. Of these, carbonates such as ethylene carbonate (EC), diethyl carbonate (DEC), dimethyl carbonate (DMC), and ethyl methyl carbonate (EMC) can be preferably used. As the supporting salt, lithium salts such as LiPF ₆ and LiBF ₄ can be preferably used.
The nonaqueous electrolytic solution may contain various additives in addition to the nonaqueous solvent and the supporting salt described above. Examples of such additives include gas generating agents such as cyclohexylbenzene (CHB) and biphenyl (BP); vinylene carbonate (VC), vinyl ethylene carbonate (VEC), fluoroethylene carbonate (FEC), lithium bis (oxalato) borate ( Examples thereof include film forming agents such as Li [B (C ₂ O ₄ ) ₂ ]).

The lithium ion secondary battery 100 as shown in FIGS. 1 to 3 includes, for example, the following steps:
(1) The long positive electrode 10 and the long negative electrode 20 longer than the positive electrode are stacked via the separator 40, and wound in the longitudinal direction to produce a flat wound electrode body 80. about;
(2) accommodating the wound electrode body 80 in the square case 50;
(3) Injecting a non-aqueous electrolyte into the square case 50;
(4) An initial charging process is performed between the positive electrode 10 and the negative electrode 20;
Can be manufactured by. Hereinafter, each process is demonstrated in order.

In the manufacturing method disclosed herein, first, a long positive electrode 10, a long negative electrode 20 longer than the positive electrode, and a separator 40 as an insulating layer are prepared. As the positive electrode 10, the negative electrode 20, and the separator 40, those already described above can be used.
Next, the separator 40, the negative electrode 20, the separator 40, and the positive electrode 10 are laminated in this order and wound in the longitudinal direction to produce a wound electrode body. At this time, at the start end in the winding direction, the negative electrode start end 21 is protruded more to the winding center side in the winding direction than the positive electrode start end 11, thereby adjusting the negative electrode remainder 22. For example, two separators 40 are wound around a core to some extent (typically about 0.5 to 2 turns) in advance, and the negative electrode 20 is sandwiched between the two separators 40 to a certain extent (typically Specifically, the remainder 22 of the negative electrode as shown in FIG. 3 is formed. Next, the positive electrode 10 may be sandwiched between the two separators 40 so that the positive and negative electrodes are insulated.
In addition, as a method of forming the wound electrode body into a flat shape, for example, a winding core having a flat cross section in the vertical direction of the winding axis may be wound so as to be flat. Alternatively, a cylindrical wound electrode body may be formed using a winding core having a substantially circular cross section in the vertical direction of the winding axis, and then pressed from the side surface to be formed into a flat shape. Thereby, the flat wound electrode body 80 can be produced.

  In a preferred embodiment, the winding or the pressing is performed so that the starting end portion 11 of the positive electrode in the winding direction is disposed on the winding flat portion of the flat wound electrode body 80. In a more preferred aspect, the winding or the starting end portion 11 in the winding direction of the positive electrode and the starting end portion 21 in the winding direction of the negative electrode are arranged on the winding flat portion of the flat wound electrode body 80. The above pressing is performed. In other words, the winding or the pressing is performed so that the negative electrode surplus portion 22 on the start end side is disposed on the wound flat portion of the flat wound electrode body 80. Thereby, loss of an active material layer (for example, a positive electrode active material layer) can be suitably prevented, and a defect rate in a manufacturing process can be reduced. Furthermore, even when the active material layer (typically, the positive electrode active material layer) repeatedly expands and contracts due to charge and discharge, excellent durability can be realized.

In the manufacturing method disclosed herein, subsequently, the wound electrode body 80 is accommodated in the square case 50. As the square case 50, the above-described materials can be used. Typically, after the wound electrode body 80 is accommodated in the case main body 52, the lid 54 is put on the opening of the case main body 52 and sealed. The sealing process between the case body 52 and the lid can be performed in the same manner as in the production of a conventional lithium ion secondary battery.
The direction (orientation) when the wound electrode body 80 is accommodated in the square case 50 is, for example, as shown in FIGS. 1 to 3, one of the two wound R portions of the wound electrode body (lower R). Part) may be arranged so as to be positioned at the bottom of the rectangular case 50 in the vertical direction. Thereby, the start end portion 81 in the winding direction of the wound electrode body can be accurately arranged in a region where the surplus non-aqueous electrolyte 60 exists. Alternatively, one of the two wound flat portions 84 of the wound electrode body may be disposed so as to be positioned at the bottom of the square case 50 in the vertical direction.
The tip of the start end 11 in the winding direction of the positive electrode is preferably arranged so as to face the lower side in the vertical direction. Thereby, the start end portion 81 (in other words, the start end portion 11 of the positive electrode and the start end portion 21 of the negative electrode) in the winding direction of the wound electrode body 80 is accurately disposed in a region where the surplus non-aqueous electrolyte 60 exists. be able to.

  In the manufacturing method disclosed herein, subsequently, a nonaqueous electrolytic solution is injected (arranged) into the square case 50. Typically, after injecting (arranging) a nonaqueous electrolyte from an injection port provided on the lid, the injection port is hermetically sealed. As the non-aqueous electrolyte, those already described above can be used. In addition, the amount of the nonaqueous electrolyte solution injected is such that the wound electrode body 80 is impregnated with the nonaqueous electrolyte solution, and the surplus nonaqueous electrolyte solution 60 is placed in the gap between the wound electrode body 80 and the square case 50. It is sufficient that the amount of the negative electrode remaining portion 24 on the start end side is located below the liquid surface 62 of the surplus non-aqueous electrolyte in the vertical direction. Thus, the lithium ion secondary battery 100 as shown in FIGS. 1 to 3 can be constructed (assembled).

  In a preferred embodiment, a gas generating agent is included in the non-aqueous electrolyte. Thereby, in the battery provided with the current interruption mechanism, the current interruption mechanism can be operated earlier at the time of overcharge. Therefore, a battery excellent in reliability (overcharge resistance) can be realized.

  Further, in the accommodation of the wound electrode body, a battery (FIG. 5) is arranged such that one of the two wound R parts (the lower R part) of the wound electrode body is located at the bottom in the vertical direction of the rectangular case 50. 1 to 3), it is preferable to adjust the injection amount of the nonaqueous electrolyte so that the level of the surplus nonaqueous electrolyte 62 is positioned at the wound flat portion 84.

The accommodation of the wound electrode body 80 and the injection of the nonaqueous electrolytic solution are typically performed in a dry air atmosphere using a dry bench, a dry room, or the like. Thereby, productivity and work efficiency can be remarkably improved compared with the case where accommodation work or liquid injection work is performed in an inert gas (for example, nitrogen gas) atmosphere using a glove box etc., for example. Furthermore, it is preferable also from a viewpoint of cost.
In general, when a large amount of oxygen is contained in the square case 50, for example, in the remainder 22 of the negative electrode of the wound electrode body 80, precipitation of a metal derived from the positive electrode active material may occur. However, according to the technique disclosed herein, such metal deposition can be suitably suppressed, and productivity and battery performance (typically, reduction in self-discharge amount) can be achieved at a high level.

In the manufacturing method disclosed herein, an initial charging process is subsequently performed between the positive electrode 10 and the negative electrode 20. Typically, an external power source is connected between the positive electrode 10 (positive electrode terminal 70) and the negative electrode 20 (negative electrode terminal 74), charged to a predetermined voltage (typically constant current charging), and then predetermined in a high temperature range. Hold for a period of (aging, leaving). Thereby, the coating film derived from the non-aqueous electrolyte can be formed on the surface of the negative electrode, and a battery having excellent cycle characteristics can be realized.
The charging voltage between the positive and negative terminals is preferably a voltage range that can be shown when the SOC is in the range of 65% to 110%, for example. For example, in a battery that is fully charged at 4.2 V, the voltage between the positive and negative electrodes may be set in a range of approximately 3.8 V to 4.3 V. The temperature during aging may be about 40 ° C. or higher (typically 50 ° C. or higher, preferably 60 ° C. or higher, for example 60 ± 10 ° C.). Moreover, the period (time) hold | maintained in a high temperature range is 5 hours-48 hours, for example, Preferably it is good to set to 10 hours-24 hours.

  In the manufacturing method disclosed herein, the initial charging process is performed in a state where the surplus portion 22 of the negative electrode on the start end side is disposed below the liquid surface 62 of the surplus nonaqueous electrolyte. Thereby, it can prevent that the electric potential of the start end part 11 of the winding direction of a positive electrode becomes high locally, and can suppress metal elution from a positive electrode active material effectively. Therefore, generation | occurrence | production of a micro short circuit can be suppressed highly and a reliable lithium ion secondary battery can be manufactured stably. This is also preferable from the viewpoint of improving the defective rate in the manufacturing process and reducing the cost.

The non-aqueous secondary battery (typically a lithium ion secondary battery) disclosed herein can be used for various applications, but is characterized by high battery performance (for example, energy density) and excellent reliability. . For example, the self-discharge amount is reduced, the initial battery capacity is high, and high durability can be realized even when charging and discharging are repeated. Furthermore, the current interrupting mechanism can be operated accurately during overcharging, and both durability (overcharge resistance) and battery characteristics (high energy density) can be achieved. Therefore, taking advantage of such properties, it can be preferably applied to a large battery in which high output and high capacity characteristics are particularly required.
Specifically, for example, it is a large capacity type lithium ion secondary battery having a theoretical capacity of 10 Ah or more (for example, 10 Ah to 250 Ah), for example, 50 Ah or more, and further 100 Ah or more (for example, 100 Ah to 200 Ah). For example, it can be preferably applied to a lithium ion secondary battery expected to be used in a charge / discharge cycle including a high rate discharge of 5C to 50C), for example, 10C or more (for example, 10C to 40C). And the lithium ion secondary battery (it may be a form of an assembled battery) of such a structure can be suitably used as a power source (drive power source) for a motor mounted on a vehicle, for example. The type of vehicle is not particularly limited, but typically includes automobiles such as plug-in hybrid cars (PHV), hybrid cars (HV), electric cars (EV), and the like.

  Hereinafter, some examples relating to the present invention will be described, but the present invention is not intended to be limited to such examples.

≪Lithium ion secondary battery A≫
Here, a lithium ion secondary battery as schematically shown in FIG. 3 was constructed. Specifically, first, Li [Ni _0.33 Co _0.33 Mn _0.33 ] O ₂ powder (LNCM) powder as a positive electrode active material powder, acetylene black (AB) as a conductive material, and a binder A slurry-like composition is prepared by mixing polyvinylidene fluoride (PVdF) with N-methylpyrrolidone (NMP) such that the mass ratio of these materials is LNCM: AB: PVdF = 94: 3: 3. did. This composition was applied to both sides of a long aluminum foil (positive electrode current collector) having a thickness of about 15 μm in a strip shape with a width of 94 mm, and then dried (drying temperature 80 ° C., 1 minute) to form a positive electrode active material layer. Formed. By rolling this with a roll press machine, a long positive electrode (total thickness: 170 μm, length: 4500 mm) was produced.

  Next, carbon black powder (C) as a negative electrode active material, styrene butadiene rubber (SBR) as a binder, and carboxymethyl cellulose (CMC) as a thickener, the mass ratio of these materials is C: SBR. : CMC = 98.3: 1.0: 0.7 was mixed with ion-exchanged water to prepare a slurry composition. This composition was applied to both sides of a long copper foil (negative electrode current collector) having a thickness of about 10 μm in a strip shape with a width of 100 mm, and then dried (drying temperature 120 ° C., 1 minute) to form a negative electrode active material layer. Formed. By rolling this with a roll press, a long negative electrode (total thickness 150 μm, length 4550 mm) longer than the positive electrode was produced.

The long positive electrode and the long negative electrode produced above were overlapped and wound through a separator to produce a flat wound electrode body. At the time of lamination of the positive electrode and the negative electrode, the production conditions were adjusted such that the remainder of the negative electrode was 40 mm at the start end in the winding direction of the wound electrode body. That is, the end of the wound electrode body in the winding direction is 10 mm (that is, (the length of the negative electrode in the longitudinal direction) − (the length of the positive electrode in the longitudinal direction) − (the length of the negative electrode surplus portion at the starting end). )) = 4550 mm−4500 mm−40 mm = 10 mm). Moreover, it adjusted so that the starting end part of a positive electrode might be arrange | positioned at the winding flat part. As a separator, alumina (Al ₂ O ₃ ) particles and an acrylic resin as a binder are formed on one surface of a three-layer base material in which a polypropylene (PP) layer is laminated on both sides of a polyethylene (PE) layer. The thing provided with the porous heat-resistant layer containing was used. And the positive electrode terminal was joined to the edge part of the positive electrode collector of the obtained winding electrode body, and the negative electrode terminal was joined to the edge part of the negative electrode collector, respectively.

The wound electrode body was accommodated in an aluminum square case, and a non-aqueous electrolyte was injected. At this time, the injection amount of the non-aqueous electrolyte is such that the non-aqueous electrolyte is impregnated in the wound electrode body, and the surplus non-aqueous electrolyte is in the gap between the wound electrode body and the square case. It is an amount present, and the height of the square case is ½ that the surplus part of the negative electrode on the start end side is below the liquid level of the surplus nonaqueous electrolyte solution in the vertical direction. It was adjusted. The non-aqueous electrolyte is supported by a mixed solvent containing ethylene carbonate (EC), dimethyl carbonate (DMC), and ethyl methyl carbonate (EMC) in a volume ratio of EC: DMC: EMC = 3: 3: 4. LiPF ₆ as a salt is dissolved at a concentration of 1 mol / L, and vinylene carbonate is added at a rate of 0.75% by mass of the whole non-aqueous electrolyte, and cyclohexylbenzene is added at a rate of 1% by mass at a rate of 4% by mass. And biphenyl added thereto, respectively. Then, a lid is attached to the opening of the square case and welded to join the lithium ion secondary battery A (capacity ratio of positive and negative electrodes (C _N / C _P ); 1.36, rated capacity; 25Ah) was constructed.

≪Lithium ion secondary battery B≫
Here, a lithium ion secondary battery 100b as schematically shown in FIG. 5 was constructed. Specifically, first, similarly to the lithium ion secondary battery A, the wound electrode body 80b was accommodated in the rectangular case 50b. At this time, the start end portion 81b (specifically, the positive electrode start end portion 11b and the negative electrode start end portion 21b) and the terminal end portion 83b (specifically, the positive electrode end portion 13b and the positive electrode end portion 11b) The negative terminal portions 23b) are arranged so as to be higher than ½ of the height of the square case 50b. Next, the non-aqueous electrolyte was poured to a height that was 1/2 that of the square case 50b. That is, the end of the wound electrode body 80b was arranged so as not to be immersed in the surplus non-aqueous electrolyte 60b (to be above the liquid surface 62b of the non-aqueous electrolyte in the vertical direction). Thus, the lithium ion secondary battery B (volume ratio of positive and negative electrodes _{(C N / C P);} 1.36, rated capacity; 25 Ah) was fabricated.

≪Initial charging process≫
The lithium ion secondary batteries A and B constructed as described above were sandwiched with a jig and pressed and restrained so that the restraining pressure was 400 kgf. Next, constant current charging / discharging was performed until the battery voltage reached 3.95 V at a constant current of 20 A, and then constant voltage charging was performed until the current reached 0.1 A at that voltage. Then, a lithium ion secondary battery whose battery voltage is adjusted to 3.95 V is placed in a temperature-controlled thermostat, the temperature is raised to 66 ° C., and high temperature aging treatment is performed until the elapsed time from the start of temperature rise reaches 20 hours. Went. After the aging lithium ion secondary battery was cooled to room temperature, constant current charge / discharge was performed until the battery voltage reached 3.0 V at a constant current of 60 A, and the SOC was adjusted to 0%.

≪Analysis of eluted metal elements≫
The lithium ion secondary batteries A and B after the initial charging treatment were disassembled, and the negative electrode and the separator facing the starting end of the positive electrode were cut out. Then, after lightly washing 2 to 3 times with a non-aqueous solvent (EC: DMC: EMC = 1: 1: 1 mixed solvent), punched out to 1 cm ² and used for ICP (Inductively Coupled Plasma) analysis. A sample was obtained. Each analytical sample was dissolved in an acid solvent (here, sulfuric acid) by heating, and the solution was analyzed by ICP-AES (Atomic Emission Spectrometry) to quantify the content (μg) of the metal element. Then, the metal elution amount (μg / cm ² ) per unit area was calculated by dividing the obtained quantitative value by the area (cm ² ) of the measurement sample. The results are shown in Table 1 and FIG.

  As shown in Table 1 and FIG. 6, in the lithium ion secondary battery A, the amount of eluted metal was reduced as compared with the lithium ion secondary battery B. Therefore, for the lithium ion secondary battery A, a battery having the same configuration was newly constructed, and further investigation was attempted by increasing the set temperature during high-temperature aging to 80 ° C. The results are shown in Table 1 and FIG. As shown in Table 1 and FIG. 6, in the lithium ion secondary battery having the configuration disclosed herein, the elution of the metal element from the positive electrode active material is greatly increased even when exposed to an extremely high temperature environment. It was found that it can be suppressed. Such results indicate the technical significance of the present invention.

  In addition, for the negative electrode and the separator facing the terminal portion of the positive electrode, the elution metal element was quantified by ICP analysis in the same manner as described above, but the measured amount of the eluted metal was relatively lower than the starting end portion ( For example, the value was about 1/5 or less.

  As mentioned above, although this invention was demonstrated in detail, the said embodiment and Example are only illustrations and what changed and changed the above-mentioned specific example is contained in the invention disclosed here.

DESCRIPTION OF SYMBOLS 10 Long-form positive electrode 11, 11a, 11b Positive electrode start-end part 13, 13a, 13b Positive electrode end-of-winding part 20 Long-form negative electrode 21, 21a, 21b Negative electrode start-end of winding direction Portions 22 and 22a Negative electrode surplus portions 23, 23a and 23b Negative electrode winding end portions 24 and 24a Negative electrode surplus portion 30 Current blocking mechanism 40 Separator 42 Separator surplus on start end side Portion 44 The remaining portion 50, 50a, 50b of the separator on the terminal end side Square case 52 Case body 54 Lid 55 Safety valve 60, 60a, 60b Excess nonaqueous electrolyte solution 62, 62a, 62b Nonaqueous electrolyte interface 70 Positive electrode Terminal 72 Negative electrode terminal 74 Positive electrode current collector plate 76 Negative electrode current collector plates 80, 80 a, 80 b Flat wound electrode bodies 81, 81 a, 81 b Start end portion 82 in the winding direction of the wound electrode body R part)
83, 83a, 83b End portion 84 in the winding direction of the wound electrode body Winding flat portion 86 Winding R portion (upper R portion)
100, 100a, 100b Lithium ion secondary battery

Claims (8)

A flat-shaped wound electrode body in which a long positive electrode and a long negative electrode longer than the positive electrode are laminated via a separator and wound in the longitudinal direction, and a non-aqueous electrolyte solution are a rectangular case A lithium ion secondary battery housed in
The wound electrode body has a remainder of the negative electrode protruding at the winding center side in the winding direction from the positive electrode at the start end in the winding direction on the winding center side,
In the gap between the wound electrode body and the square case, an excess non-aqueous electrolyte exists,
The surplus portion of the negative electrode on the start end side is disposed in a region where the excess non-aqueous electrolyte is present when the battery is disposed at a predetermined position in a predetermined posture ,
The flat wound electrode body has two wound flat portions facing each other, and two semicircular wound R portions interposed between the two wound flat portions,
One of the two wound R portions is disposed on the bottom in the vertical direction of the square case,
The lithium ion secondary battery in which the liquid level of the surplus nonaqueous electrolytic solution is disposed on the wound flat portion . The wound electrode body has a remainder of the negative electrode that protrudes to the outer periphery of the winding in the winding direction from the positive electrode at the end of the winding direction on the outer periphery of the winding.
2. The lithium ion secondary battery according to claim 1, wherein a surplus portion of the negative electrode on the terminal end side is disposed in a region where the surplus nonaqueous electrolyte is present. Before SL start portion of the wound direction of the positive electrode is disposed on the winding flat portion, a lithium ion secondary battery according to claim 1 or 2. The lithium ion secondary battery according to any one of claims 1 to 3, wherein a surplus portion of the negative electrode on the start end side is disposed in the wound flat portion. A current interruption mechanism that operates when the pressure in the rectangular case rises;
The lithium ion secondary battery according to any one of claims 1 to 4, further comprising a gas generating agent that decomposes to generate gas when the battery is overcharged.   6. The device according to claim 1, wherein when the battery is disposed in a predetermined position at a predetermined position, a tip of a start end portion in a winding direction of the positive electrode faces a lower side in a vertical direction. The lithium ion secondary battery as described. A flat-shaped wound electrode body in which a long positive electrode and a long negative electrode longer than the positive electrode are laminated via a separator and wound in the longitudinal direction, and a non-aqueous electrolyte solution are a rectangular case A method of manufacturing a lithium ion secondary battery housed in
Laminating the long positive electrode and the long negative electrode longer than the positive electrode through the separator, and winding in the longitudinal direction to produce a flat wound electrode body, The wound electrode body has a remainder of the negative electrode that protrudes toward the winding center in the winding direction from the positive electrode at the start end in the winding direction on the winding center side;
Accommodating the wound electrode body in the square case;
Injecting the non-aqueous electrolyte into the rectangular case in which the wound electrode body is accommodated, wherein the amount of the non-aqueous electrolyte is injected into the wound electrode body by the non-aqueous electrolysis. An amount of surplus non-aqueous electrolyte in the gap between the wound electrode body and the square case that is impregnated with the liquid, and the surplus portion of the negative electrode on the start end side is the surplus non-aqueous electrolyte. Determined to be vertically below the electrolyte level; and
Performing an initial charging process between the positive electrode and the negative electrode in a state in which the surplus portion of the negative electrode on the start end side is disposed below the liquid surface of the surplus nonaqueous electrolyte solution in the vertical direction;
It encompasses,
The flat wound electrode body has two wound flat portions facing each other, and two semicircular wound R portions interposed between the two wound flat portions,
When the wound electrode body is accommodated in the rectangular case, one of the two wound R portions is disposed so as to be positioned at the bottom in the vertical direction of the rectangular case,
The pouring amount of the non-aqueous electrolyte, the nonaqueous electrolyte liquid surface height of the surplus Ru is determined to be located in said winding flat portion, a manufacturing method of a lithium ion secondary battery. The wound electrode body, the wound the flat portion beginning of winding direction of the positive electrode is wound to be placed, the production method of the lithium ion secondary battery according to claim 7.

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